NM_000432.4(MYL2):c.456C>T (p.Tyr152=) AND Cardiomyopathy
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Apr 28, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000777833.10
Allele description [Variation Report for NM_000432.4(MYL2):c.456C>T (p.Tyr152=)]
NM_000432.4(MYL2):c.456C>T (p.Tyr152=)
Condition(s)
- Name:
- Cardiomyopathy (CMYO)
- Synonyms:
- Cardiomyopathies
- Identifiers:
- MONDO: MONDO:0004994; MedGen: C0878544; Human Phenotype Ontology: HP:0001638
Assertion and evidence details
Last Updated: Jul 29, 2024